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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01344668
Other study ID # 101523
Secondary ID 1R18DK083264-01A
Status Completed
Phase N/A
First received April 27, 2011
Last updated October 12, 2016
Start date May 2011
Est. completion date May 2016

Study information

Verified date October 2016
Source Vanderbilt University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary hypotheses are that the intervention will improve A1C, blood pressure, lipids, weight, self-efficacy, self-management behaviors, and use of clinical services at 12 and 24 months follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 411
Est. completion date May 2016
Est. primary completion date May 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Patient has a clinical diagnosis of Type 2 Diabetes

- Age 18-85 years

- English or Spanish speaking

- Most recent A1C = 7.5%

- Patient agrees to participate in the study for the full two years duration.

Exclusion Criteria:

- Poor visual acuity (vision worse than 20/50 using Rosenbaum Pocket Screener) -- Significant dementia or psychosis (by health provider report or chart review)

- Terminal illness with anticipated life expectancy < 2 years (per health provider or patient report).

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
Enhanced Diabetes Education
Provide enhanced diabetes education
Standard Diabetes Education
Provide Standard Diabetes Education

Locations

Country Name City State
United States Vanderbilt University Nashville Tennessee

Sponsors (2)

Lead Sponsor Collaborator
Vanderbilt University National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in A1C at 12 months The primary outcome will be the improvement in A1C at 12 months between Intervention group patients and Control group patients. 12 months No
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